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  • 1
    ISSN: 1365-2478
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Geosciences , Physics
    Notes: Known mineral occurrences in northern Vancouver Island are typically hosted in volcanic units of the Bonanza Group. At a local scale, the mineralization is associated with advanced argillic bedrock alteration and is often intimately related to porphyry intrusions. On a larger scale, faults are thought to exert the most significant control on the distribution of mineralized host rocks. Poor exposures and a complex glacial history limit the use of traditional methods of geological mapping and mineral exploration in this region and to date geophysical methods have been under-utilized. Here we present findings from four standard geophysical (gravity, magnetics, electromagnetics and seismic refraction) methods, recently deployed here to elucidate the subsurface geology, as well as to identify new targets for base metal exploration.Results at two different sites show that the integrated interpretation of geophysical data, constrained by physical rock property measurements, yields detailed images of the subsurface at a fraction of the cost of drilling. At one site, east of Rupert Inlet, the final subsurface model shows that the Bonanza Group is not nearly as extensive as previously presumed. An extension of the Holberg Fault is identified some 50 km east of the visibly mapped outcrop and an extensive zone of alteration around the fault is recognized. Furthermore, a number of the methods provide support for the existence of a porphyry dike at this site. At the second site, north of Rupert Inlet, magnetic and electromagnetic data prove effective at mapping alteration and locating shear zones beneath a relatively thin drift cover. Together, these results help outline a strategy for exploration in drift-covered terrains and show that a redirection of exploration effort is warranted in the case of northern Vancouver Island.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    Industrial and engineering chemistry 9 (1937), S. 430-431 
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology , Process Engineering, Biotechnology, Nutrition Technology
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    Industrial and engineering chemistry 12 (1940), S. 229-231 
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology , Process Engineering, Biotechnology, Nutrition Technology
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    Industrial and engineering chemistry 13 (1941), S. 809-810 
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology , Process Engineering, Biotechnology, Nutrition Technology
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 104 (1996), S. 7364-7365 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 103 (1995), S. 1582-1587 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: We compare computer simulation results for the angular velocity autocorrelation function (AVACF) of a colloidal particle with theoretical predictions. We consider both spherical and nonspherical particles in two and three dimensions. The theoretical prediction for the long-time decay of the AVACF in three dimensions is well known, here we also give the two-dimensional result, along with a sketch of how it was derived. For spherical particles we find excellent agreement between the simulations results and theoretical predictions in both two and three dimensions. We also find that the same expressions apply to the nonspherical particles when the particles have had time to undergo a significant angular displacement. This observation is again in agreement with theory. © 1995 American Institute of Physics.
    Type of Medium: Electronic Resource
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  • 7
    Electronic Resource
    Electronic Resource
    Oxford, UK : Blackwell Publishing Ltd
    BJOG 68 (1961), S. 0 
    ISSN: 1471-0528
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Medicine
    Type of Medium: Electronic Resource
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  • 8
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 111 (1999), S. 8708-8720 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: In a simple model for the long-time dynamical behavior of Brownian suspensions, particles diffuse independently while simultaneously undergoing direct interactions with each other. Despite its simplicity, this model forms the basis of both the Brownian dynamics computer simulation technique and apparently successful theories. Here we use the approach to study numerically the viscoelastic response of a suspension of hard spheres. At low volume fractions (10%) we find that the frequency dependence of the viscosity is in agreement with theoretical calculations based on solving the two-particle Smoluchowski equation. At a higher volume fraction (45%) we find that the model is not well described by various extensions of low density theory that have been proposed. Including hydrodynamics in a minimal way (by allowing the particles to diffuse with the short-time diffusion coefficient) and comparing with experiment, the model successfully reproduces the viscoelastic response over an intermediate range of frequencies. However, at low frequencies a significant disagreement emerges. A "slowing down" of the dynamics of the particles at longer times, more apparent in the simulations than in the experimental results, appears to be the cause of this discrepancy. Ultimately, this leads to a significant overestimate of the zero frequency (Newtonian) viscosity. The reason theories based on the approach yield such excellent agreement with experiment, we can only conclude, is because they fail to describe the model adequately. © 1999 American Institute of Physics.
    Type of Medium: Electronic Resource
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  • 9
    ISSN: 1520-510X
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 10
    ISSN: 1089-7550
    Source: AIP Digital Archive
    Topics: Physics
    Notes: The yellow compound of stoichiometry (4-chloropyridinium)3Fe2Cl9 belongs to the space group P21/n with four formula units in the unit cell. Structural analysis shows that the iron is present as the FeX4− ion. Magnetic measurements on single crystals show that the material orders as a canted antiferromagnet at 2.725 K. Replacement of the 4-chloro cation by the 4-bromo analog yields an isomorphous material and shifts the transition temperature to 2.34 K. The phase diagrams of both salts have also been determined. For [(4-chloropyridinium)FeCl4]2⋅4-chloropyridinium chloride, the bicritical point is at 2.40 K and 7 kOe, and HSF(0)=5.5 kOe. With Hc(0)=56 kOe, α=HA/HE=1.9×10−2. In the case of [(4-bromopyridinium)FeCl4]2⋅4-bromopyridinium chloride, HSF(0)=3 kOe, Hc(0)=42 kOe, α=1.0×10−2, and the bicritical point is at 2.24 K and 4.2 kOe. Crystallographic investigations at 25 K are reported on the isomorphous (4-chloropyridinium)3Fe2Br9 and on (4-bromopyridinium)3Fe2Cl1.3Br7.7. Magnetic measurements on single crystals show that (4-bromopyridinium)3Fe2Cl1.3Br7.7 orders as a canted antiferromagnet at 5.67 K, while (4-chloropyridinium)3Fe2Br9 orders similarly at 7.96 K. These compounds behave approximately as S=5/2, three-dimensional Heisenberg antiferromagnets.
    Type of Medium: Electronic Resource
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